Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07725978

Contrology Training in Patients With Non-Specific Neck Pain

This randomized controlled trial will evaluate the effects of a 12-week Contrology training program in patients with non-specific neck pain. Participants will be randomly allocated into two groups. The experimental group will receive Contrology training, while the control group will receive conventional physiotherapy. Outcomes will include pain intensity, cervical range of motion, neck-related disability, and craniovertebral angle. Assessments will be performed at baseline, 4 weeks, 8 weeks, and 12 weeks. The study aims to determine whether Contrology training is more effective than conventional physiotherapy in improving pain, posture, mobility, and functional disability in adults with non-specific neck pain.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Maqbool memorial hospital, Shakargarh.

Shakargarh, Punjab Province, Pakistan

Location contact

Muhammad Ali

CONTACT

[email protected]

03000467607

About this study

Non-specific neck pain is a common musculoskeletal condition that may lead to pain, restricted cervical movement, functional disability, and altered head and neck posture. Forward head posture, commonly assessed through craniovertebral angle, is frequently associated with neck pain and may contribute to increased mechanical load on cervical structures. Exercise-based rehabilitation is commonly used for the management of non-specific neck pain; however, the effects of Contrology training on pain, cervical range of motion, disability, and craniovertebral angle require further investigation.

This study is designed as a single-center, two-arm, parallel-group randomized controlled trial. A total of 40 participants with non-specific neck pain will be recruited and randomly allocated into two equal groups. Group A will receive Contrology training, and Group B will receive conventional physiotherapy. The intervention period will be 12 weeks. Participants will be assessed at baseline, 4 weeks, 8 weeks, and 12 weeks.

The primary outcome will be craniovertebral angle, measured using standardized lateral-view digital photography. Secondary outcomes will include pain intensity measured by the Numeric Pain Rating Scale, neck-related disability measured by the Neck Disability Index, and cervical range of motion measured using a digital inclinometer and/or universal goniometer. The study will compare changes within each group over time and between groups to determine the effectiveness of Contrology training compared with conventional physiotherapy.

These points match your thesis protocol: randomized trial, 40 participants, Contrology versus conventional physiotherapy, and outcomes including NPRS, NDI, CVA, and cervical ROM assessed across baseline, 4, 8, and 12 weeks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Inclusion Criteria:
  • Adults aged 18 to 40 years.
  • Participants diagnosed with non-specific neck pain.
  • Neck pain duration of at least 4 weeks.
  • Numeric Pain Rating Scale score of at least 3 out of 10.
  • Craniovertebral angle less than 49 degrees.
  • Participants willing to provide informed consent and attend the treatment sessions.

Exclusion criteria

  • Cervical radiculopathy or myelopathy.
  • Cervical spinal stenosis.
  • History of cervical spine fracture, trauma, or surgery.
  • Inflammatory joint disease or systemic rheumatologic disorder.
  • Neurological disorders affecting neck movement or posture.
  • Vestibular disorders or severe balance problems.
  • Any serious medical condition preventing participation in exercise-based treatment.
  • Current participation in another neck pain rehabilitation program.

Treatment and study plan

Contrology Training

Other

Contrology training is a Pilates-based exercise program emphasizing concentration, control, centering, breathing, precision, and flowing movement. Participants will perform supervised exercises targeting postural correction, cervical and thoracic mobility, deep cervical flexor activation, scapular stabilization, core control, and controlled breathing for 12 weeks.

Conventional Physiotherapy

Other

Conventional physiotherapy will include routine exercise-based management for non-specific neck pain, including cervical range of motion exercises, stretching, strengthening exercises, postural correction, and patient education. Treatment will be provided for 12 weeks.

Primary outcomes

  1. Craniovertebral Angle

    Time frame: Baseline, 4 weeks, 8 weeks, and 12 weeks

    Craniovertebral angle will be measured using standardized lateral-view digital photography. The angle will be calculated between a horizontal line passing through the C7 spinous process and a line connecting C7 to the tragus of the ear. A higher craniovertebral angle indicates improved head and neck posture, while a lower angle indicates greater forward head posture.

Secondary outcomes

  1. Numeric Pain Rating Scale

    Time frame: Baseline, 4 weeks, 8 weeks, and 12 weeks

    Pain intensity will be measured using the Numeric Pain Rating Scale. Participants will rate their neck pain on a scale from 0 to 10, where 0 indicates no pain and 10 indicates the worst possible pain. A lower score indicates less pain.

  2. Neck Disability Index

    Time frame: Baseline, 4 weeks, 8 weeks, and 12 weeks

    Neck-related disability will be measured using the Neck Disability Index. The questionnaire includes 10 sections related to pain and daily activities. Higher scores indicate greater neck-related disability, while lower scores indicate less disability.

  3. Cervical Range of Motions

    Time frame: Baseline, 4 weeks, 8 weeks, and 12 weeks

    These will be assessed with a Universal goniometer

Study contacts

Contact information is provided by the study sponsor or research team.

Amna Zia, PhD*

CONTACT

[email protected]

03244686993

Samrood Akram, PhD*

CONTACT

[email protected]

03324806143

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Effects of Contrology Training on Pain, Cervical Range of Motion, Disability, and Craniovertebral Angle in Patients With Non-Specific Neck Pain

Acronym: CT-NSNP

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jul 24, 2026
Registry last updated
Jul 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.